salicylic acid has been researched along with Syndrome in 190 studies
Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Endocrinological examination by insulin-induced hypoglycemia showed not only the presence of GH deficiency, but also the loss of the glucagon secretion response to hypoglycemia." | 7.72 | Johanson-blizzard syndrome: loss of glucagon secretion response to insulin-induced hypoglycemia. ( Enoki, M; Fujishima, M; Takada, G; Takahashi, T; Tsuchida, S, 2004) |
| " Endocrinological examination by insulin-induced hypoglycemia showed not only the presence of GH deficiency, but also the loss of the glucagon secretion response to hypoglycemia." | 3.72 | Johanson-blizzard syndrome: loss of glucagon secretion response to insulin-induced hypoglycemia. ( Enoki, M; Fujishima, M; Takada, G; Takahashi, T; Tsuchida, S, 2004) |
| "There are multiple types of dysesthesias depending on the body location and the nerves involved." | 2.53 | Neurocutaneous disease: Neurocutaneous dysesthesias. ( Cole, E; Fernandez, KH; Shumway, NK, 2016) |
| "While pulmonary hypertension is usually not associated with AOS, the abnormal endothelial regulation of vascular tone seen in the pulmonary vasculature may enhance current pathophysiologic concepts of vascular abnormalities in AOS." | 2.42 | A case of Adams-Oliver syndrome with associated brain and pulmonary involvement: further evidence of vascular pathology? ( Blackston, D; Piazza, AJ; Sola, A, 2004) |
| "Now, he is 3 years old, and has microcephaly, moderate mental retardation, left spastic hemiplegia, and epilepsy." | 2.41 | A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation. ( Caksen, H; Kurtoğlu, S, 2000) |
| "Multiple skin cylindromas are of autosomal dominant transmission and may be associated with spiradenoma and trichoepithelioma." | 1.40 | [CO2 laser treatment of skin cylindromas in Brooke-Spiegler syndrome]. ( Bénateau, H; Chevalier, JM; Dolfus, C; Dompmartin, A; Labbé, D; Richard, A; Sergent, B; Tesnière, A; Verneuil, L, 2014) |
| "Brooke-Spiegler syndrome is a rare, autosomal dominant disease characterized by multiple skin appendage tumors caused by various mutations in the CYLD gene on chromosome 16q12-q13." | 1.36 | New mutation in the CYLD gene within a family with Brooke-Spiegler syndrome. ( Enk, AH; Froster, UG; Helmbold, P; Näher, H; Nümann, A; Scholz, IM, 2010) |
| "Adams-Oliver syndrome has a wide spectrum of anomalies ranging from aplasia cutis congenita, cutis marmorata telangiectatica congenita and transverse limb defects to lethal anomalies." | 1.35 | Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome. ( Akalan, N; Bahadir, S; Bilginer, B; Onal, MB, 2008) |
| "Brooke-Spiegler syndrome is an autosomal dominant tumor predisposition disorder." | 1.35 | Brooke-Spiegler syndrome complicated by unilateral hearing loss. ( Bauer, B; Frank, J; Hamm, H; Parren, LJ, 2008) |
| "The National Foundation for Ectodermal Dysplasias convened the International Research Symposium for AEC Syndrome on November 8-10, 2006, at Texas Children's Hospital/Baylor College of Medicine, Houston, TX with appropriate IRB approval." | 1.35 | Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome. ( Bree, AF; Julapalli, MR; Scher, RK; Siegfried, EC; Sybert, VP, 2009) |
| "Adams-Oliver syndrome is a rare congenital disorder that includes congenital scalp and skull defects, variable degrees of terminal transverse limb anomalies, and cardiac malformations." | 1.35 | Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome. ( Fried, A; Khashab, ME; Khashab, YE; Nejat, F; Pierce, SD; Rhee, ST, 2009) |
| "Association of both syndromes has been reported in only one child." | 1.33 | Adams-Oliver syndrome and hepatoportal sclerosis: occasional association or common mechanism? ( Amiel, J; Fabre, M; Girard, M; Jacquemin, E; Lyonnet, S; Pariente, D, 2005) |
| "This syndrome is characterized by obesity, mild mental retardation, delayed puberty, acanthosis nigricans and hyperinsulinaemia." | 1.31 | Cutis verticis gyrata of the scalp in a patient with autosomal dominant insulin resistance syndrome. ( Black, MM; Brenton, DP; Darley, CR; Lee, PJ; Sonksen, PH; Woollons, A, 2000) |
| "The GAPO syndrome is a rare but distinct genetic disorder." | 1.31 | [GAPO syndrome]. ( Abid, R; Elandaloussi, H; Ezzine, N; Fazaa, B; Goucha, S; Jaber, K; Kamoun, MR, 2000) |
| " We describe the effectiveness of cyclosporin A in a case of GLPLS at the dosage of 4 mg/kg/day." | 1.31 | Graham Little-Piccardi-Lassueur syndrome: effective treatment with cyclosporin A. ( Bianchi, L; Carboni, I; Chimenti, S; Paro Vidolin, A; Piemonte, P, 2001) |
| "Spiradenomas and cylindromas have so many features in common that they have been regarded as polar extremes belonging to a spectrum of cutaneous adnexal neoplasms." | 1.30 | Brooke-Spiegler syndrome variant: segregation of tumor types with mixed differentiation in two generations. ( Alegre, M; de Moragas, JM; Fernández-Figueras, MT; Nadal, C; Puig, L, 1998) |
| "Buckly syndrome was suspected in the second case." | 1.30 | [Eosinophilic pustulosis in an infant accompanied by immune deficit]. ( Bourrat, E; Guibal, F; Morel, P; Prigent, F; Rybojad, M; Vignon-Pennamen, MD, 1999) |
| "The Parry-Romberg syndrome is an acquired progressive hemifacial atrophy involving the subcutaneous tissues of the scalp and face." | 1.30 | Parry-Romberg syndrome with contralateral and ipsilateral extremity involvement. ( Chapman, MS; Peraza, JE; Spencer, SK, 1999) |
| "Some patients had partial syndactyly of the 3rd and 4th fingers, and complete cutaneous syndactyly of the 2nd and 3rd toes." | 1.29 | Scalp-ear-nipple syndrome: additional manifestations. ( Edwards, MJ; McDonald, D; Moore, P; Rae, J, 1994) |
| "Hay-Wells syndrome is an autosomal dominant condition characterized by ankyloblepharon filiforme adnatum, ectodermal dysplasia, and cleft palate with or without associated cleft lip (AEC syndrome)." | 1.29 | Severe skin erosions and scalp infections in AEC syndrome. ( Stephan, MJ; Sybert, VP; Vanderhooft, SL, 1993) |
| "Rapp-Hodgkin syndrome is an autosomal dominant condition characterized by cleft lip and palate, peculiar craniofacial features, and ectodermal dysplasia, consisting of abnormalities of teeth, hair, nails and sweating." | 1.29 | Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity? ( Barbareschi, M; Cambiaghi, S; Caputo, R; Menni, S; Tadini, G, 1994) |
| "Carpenter's syndrome is a relatively rare craniofacial deformity which will occasionally present to craniofacial surgeons for treatment." | 1.29 | Surgical caution with Carpenter's syndrome. ( Poole, MD, 1993) |
| "Brooke-Spiegler syndrome is characterized by the development of multiple trichoepitheliomas and cylindromas." | 1.29 | A nevoid plaque with histological changes of trichoepithelioma and cylindroma in Brooke-Spiegler syndrome. An immunohistochemical study with cytokeratins. ( Kind, P; Plewig, G; Schirren, CG; Wörle, B, 1995) |
| "The epidermal nevus syndrome is characterized by the association of epidermal nevi with abnormalities of the skin, skeletal system, central nervous system, eyes, and cardiovascular system, as well as with malignant conditions." | 1.29 | Epidermal nevus syndrome: association with central precocious puberty and woolly hair nevus. ( Ganong, CA; Klingensmith, GJ; Tay, YK; Weston, WL, 1996) |
| "Buschke-Ollendorff syndrome is an association of connective tissue nevi and osteopoikilosis that usually appears in the first decades of life." | 1.28 | Buschke-Ollendorff syndrome of the scalp: histologic and ultrastructural findings. ( Ben-David, E; David, M; Rothem, A; Sandbank, M; Trattner, A, 1991) |
| "An electronystagmogram demonstrated periodic alternating nystagmus." | 1.27 | An association of subtotal cerebellar agenesis with organoid nevus--a possible new variety of neurocutaneous syndrome. ( Fukuyama, Y; Hara, M; Izumi, T; Kobayashi, N; Maeda, Y; Wang, PJ; Yajima, K, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 56 (29.47) | 18.7374 |
| 1990's | 51 (26.84) | 18.2507 |
| 2000's | 58 (30.53) | 29.6817 |
| 2010's | 20 (10.53) | 24.3611 |
| 2020's | 5 (2.63) | 2.80 |
| Authors | Studies |
|---|---|
| Bento, RF | 1 |
| Guatimosim, MH | 1 |
| Bensadon, Rde L | 1 |
| Sanchez, TG | 1 |
| Voegels, RL | 1 |
| Mala, L | 1 |
| Bazard, MC | 1 |
| Berrod, JP | 1 |
| Wahl, D | 1 |
| Raspiller, A | 1 |
| Jedrzejczak, M | 1 |
| Powell, MR | 1 |
| Brancaccio, G | 1 |
| Di Brizzi, EV | 1 |
| Kittler, H | 1 |
| Lallas, A | 1 |
| Longo, C | 1 |
| Malvehy, J | 1 |
| Moscarella, E | 1 |
| Pellerone, S | 1 |
| Puig, S | 1 |
| Ronchi, A | 1 |
| Thomas, L | 1 |
| Argenziano, G | 1 |
| Gessler, J | 1 |
| Tejasvi, T | 1 |
| Bresler, SC | 1 |
| Hinschberger, O | 1 |
| Bernier, C | 1 |
| Damour, AS | 1 |
| Oudeville, P | 1 |
| Kieffer, P | 1 |
| Asfour, L | 1 |
| Sinclair, R | 1 |
| Oyesanya, T | 1 |
| Boozalis, E | 1 |
| Kwatra, SG | 1 |
| Cohen, BA | 1 |
| Chandan, N | 1 |
| Lake, EP | 1 |
| Chan, LS | 1 |
| Bradburn, KH | 1 |
| Elston, D | 1 |
| Murphey, AW | 1 |
| Patel, KG | 1 |
| Divine, J | 1 |
| Rudnick, EW | 1 |
| Lien, M | 1 |
| László, FG | 1 |
| Bolaji, RS | 1 |
| Burrall, BA | 1 |
| Eisen, DB | 1 |
| Rostami, P | 1 |
| Mahmoudi, E | 1 |
| Sotoudeh, A | 1 |
| Nakhaeimoghadam, M | 1 |
| Lurkin, I | 1 |
| Zwarthoff, EC | 1 |
| Rezaei, N | 1 |
| Dubourg, G | 1 |
| Socolovschi, C | 1 |
| Del Giudice, P | 1 |
| Fournier, PE | 1 |
| Raoult, D | 1 |
| Richard, A | 1 |
| Chevalier, JM | 1 |
| Verneuil, L | 1 |
| Sergent, B | 1 |
| Tesnière, A | 1 |
| Dolfus, C | 1 |
| Labbé, D | 1 |
| Bénateau, H | 1 |
| Dompmartin, A | 1 |
| Zhao, J | 1 |
| Li, G | 1 |
| Zhang, Y | 1 |
| Zhu, X | 1 |
| Hou, K | 1 |
| Dolohanty, LB | 1 |
| Richardson, SJ | 1 |
| Herrmann, DN | 1 |
| Markman, J | 1 |
| Mercurio, MG | 1 |
| Yorulmaz, A | 1 |
| Artuz, F | 1 |
| Er, O | 1 |
| Guresci, S | 1 |
| Shumway, NK | 1 |
| Cole, E | 1 |
| Fernandez, KH | 1 |
| Schissler, C | 1 |
| Velter, C | 1 |
| Lipsker, D | 1 |
| Bilginer, B | 1 |
| Onal, MB | 1 |
| Bahadir, S | 1 |
| Akalan, N | 1 |
| Parren, LJ | 1 |
| Bauer, B | 1 |
| Hamm, H | 1 |
| Frank, J | 1 |
| Mégarbané, A | 1 |
| Slim, R | 1 |
| Nürnberg, G | 1 |
| Ebermann, I | 1 |
| Nürnberg, P | 1 |
| Bolz, HJ | 1 |
| Furumiya, J | 1 |
| Nishimura, H | 1 |
| Nakanishi, A | 1 |
| Hashimoto, Y | 1 |
| Mitsiakos, G | 1 |
| Giougi, E | 1 |
| Tsakalidis, C | 1 |
| Kourti, M | 1 |
| Chatziionnidis, H | 1 |
| Karagianni, P | 1 |
| Kolibianakis, EM | 1 |
| Nikolaidis, N | 1 |
| Rajan, N | 2 |
| Trainer, AH | 2 |
| Burn, J | 2 |
| Langtry, JA | 2 |
| Baskar, S | 1 |
| Kulkarni, ML | 1 |
| Kulkarni, AM | 1 |
| Vittalrao, S | 1 |
| Kulkarni, PM | 1 |
| Bree, AF | 2 |
| Julapalli, MR | 1 |
| Scher, RK | 1 |
| Sybert, VP | 2 |
| Siegfried, EC | 1 |
| Bochukova, EG | 1 |
| Soneji, S | 1 |
| Wall, SA | 1 |
| Wilkie, AO | 1 |
| Wolfe, SQ | 1 |
| Farhat, H | 1 |
| Elhammady, MS | 1 |
| Moftakhar, R | 1 |
| Aziz-Sultan, MA | 1 |
| Ashworth, A | 1 |
| Roberts, C | 1 |
| Chapman, P | 1 |
| Khashab, ME | 1 |
| Rhee, ST | 1 |
| Pierce, SD | 1 |
| Khashab, YE | 1 |
| Nejat, F | 1 |
| Fried, A | 1 |
| Arndt, S | 1 |
| Aschendorff, A | 1 |
| Schild, C | 1 |
| Beck, R | 1 |
| Maier, W | 1 |
| Laszig, R | 1 |
| Birkenhäger, R | 1 |
| Scholz, IM | 1 |
| Nümann, A | 1 |
| Froster, UG | 1 |
| Helmbold, P | 1 |
| Enk, AH | 1 |
| Näher, H | 1 |
| O'Blenes, CA | 1 |
| Lee, JP | 1 |
| Walsh, NM | 1 |
| Morris, SF | 1 |
| Friedrich, RE | 1 |
| Zegarska, B | 1 |
| Kallas, D | 1 |
| Schwartz, RA | 1 |
| Czajkowski, R | 1 |
| Uchanska, G | 1 |
| Placek, W | 1 |
| Becker, R | 1 |
| Kunze, J | 1 |
| Horn, D | 1 |
| Gasiorek-Wiens, A | 1 |
| Entezami, M | 1 |
| Rossi, R | 1 |
| Guschmann, M | 1 |
| Sarioglu, N | 1 |
| Plottova-Puech, I | 1 |
| Vidal, C | 1 |
| Godard, W | 1 |
| Cambazard, F | 1 |
| ROSENTHAL, JW | 1 |
| KLOEPFER, HW | 1 |
| MIROSHNICHENKO, VA | 1 |
| Urbani, CE | 1 |
| Hill, CJ | 1 |
| Lane, CM | 1 |
| Long, C | 1 |
| Clarke, A | 1 |
| Pilz, DT | 1 |
| Federici, S | 1 |
| Griffiths, D | 1 |
| Siberchicot, F | 1 |
| Chateil, JF | 1 |
| Gilbert, B | 1 |
| Lacombe, D | 1 |
| Kakagia, D | 1 |
| Lambropoulou, M | 1 |
| Alexiadis, G | 1 |
| Taniai, H | 1 |
| Chen, H | 1 |
| Ursin, S | 1 |
| Patel, MS | 1 |
| Taylor, GP | 1 |
| Bharya, S | 1 |
| Al-Sanna'a, N | 1 |
| Adatia, I | 1 |
| Chitayat, D | 1 |
| Suzanne Lewis, ME | 1 |
| Human, DG | 1 |
| Piazza, AJ | 1 |
| Blackston, D | 1 |
| Sola, A | 1 |
| Takahashi, T | 1 |
| Fujishima, M | 1 |
| Tsuchida, S | 1 |
| Enoki, M | 1 |
| Takada, G | 1 |
| Baris, H | 1 |
| Tan, WH | 1 |
| Kimonis, VE | 1 |
| Sng, KW | 1 |
| Salyer, KE | 1 |
| Barcelo, CR | 1 |
| Girard, M | 1 |
| Amiel, J | 2 |
| Fabre, M | 2 |
| Pariente, D | 1 |
| Lyonnet, S | 2 |
| Jacquemin, E | 1 |
| Maniscalco, M | 1 |
| Zedda, A | 1 |
| Faraone, S | 1 |
| de Laurentiis, G | 1 |
| Verde, R | 1 |
| Molese, V | 1 |
| Lapiccirella, G | 1 |
| Sofia, M | 1 |
| Ishida, LH | 1 |
| Alves, HR | 1 |
| Munhoz, AM | 1 |
| Kaimoto, C | 1 |
| Ishida, LC | 1 |
| Saito, FL | 1 |
| Gemperlli, R | 1 |
| Ferreira, MC | 1 |
| Smith, VV | 1 |
| Anderson, G | 1 |
| Malone, M | 1 |
| Sebire, NJ | 1 |
| Sobreira, NL | 1 |
| Brunoni, D | 1 |
| Cernach, MC | 1 |
| Perez, AB | 1 |
| Pouessel, G | 1 |
| Dieux-Coeslier, A | 1 |
| Wacrenier, A | 1 |
| Gottrand, F | 1 |
| De Leo, A | 1 |
| Innocenzi, D | 1 |
| Onesti, MG | 1 |
| Potenza, C | 1 |
| Toscani, M | 1 |
| Scuderi, N | 1 |
| Sankhyan, N | 1 |
| Kaushal, RK | 1 |
| Jaswal, RS | 1 |
| Koizumi, T | 1 |
| Halpern, AV | 1 |
| Bansal, A | 1 |
| Heymann, WR | 1 |
| McLucas, P | 1 |
| Fulchiero, GJ | 1 |
| Fernandez, E | 1 |
| Miller, JJ | 1 |
| Zaenglein, AL | 1 |
| Salameh, F | 1 |
| Henig, I | 1 |
| Bar-Shalom, R | 1 |
| Maza, I | 1 |
| Kim, C | 1 |
| Kovich, OI | 1 |
| Dosik, J | 1 |
| Srivastava, M | 1 |
| Mikkilineni, R | 1 |
| Konstadt, J | 1 |
| Heras Mulero, C | 1 |
| Bartralot Soler, R | 1 |
| Rodríguez-Cano, L | 1 |
| Mollet Sánchez, J | 1 |
| Palacio Aller, L | 1 |
| Aparicio Español, G | 1 |
| Bodet Castillo, D | 1 |
| Bassas Freixas, P | 1 |
| García-Patos, V | 1 |
| Gómez-Martín, B | 1 |
| Escamilla-Martínez, E | 1 |
| Martínez-Nova, A | 1 |
| Sánchez-Rodríguez, R | 1 |
| Holmes, MD | 1 |
| Greither, A | 1 |
| Rehrmann, A | 1 |
| Wang, PJ | 1 |
| Maeda, Y | 1 |
| Izumi, T | 1 |
| Yajima, K | 1 |
| Hara, M | 1 |
| Kobayashi, N | 1 |
| Fukuyama, Y | 1 |
| Russell, LJ | 1 |
| Weaver, DD | 1 |
| Bull, MJ | 1 |
| Weinbaum, M | 1 |
| van den Bergh, P | 1 |
| Fryns, JP | 10 |
| Wilms, G | 1 |
| Piot, R | 1 |
| Dralands, G | 1 |
| van den Bergh, R | 1 |
| Miyao, M | 1 |
| Saito, T | 1 |
| Yamamoto, Y | 1 |
| Kamoshita, S | 1 |
| Stankler, L | 1 |
| Lloyd, D | 1 |
| Pollitt, RJ | 1 |
| Gray, ES | 1 |
| Thom, H | 1 |
| Russell, G | 1 |
| Bitoun, P | 1 |
| Gellis, S | 1 |
| Feingold, M | 1 |
| Bart, RS | 1 |
| Kopf, AW | 1 |
| Nielsen, T | 1 |
| Schmidt, H | 1 |
| Søgaard, H | 1 |
| Moreno Fuenmayor, H | 1 |
| Zapata, HH | 1 |
| Sletten, LJ | 1 |
| Pierpont, ME | 1 |
| Busch, S | 1 |
| Altmeyer, P | 1 |
| Edwards, MJ | 1 |
| McDonald, D | 1 |
| Moore, P | 1 |
| Rae, J | 1 |
| Bamforth, JS | 1 |
| Kaurah, P | 1 |
| Byrne, J | 1 |
| Ferreira, P | 1 |
| Farrell, SA | 1 |
| Warda, LJ | 1 |
| LaFlair, P | 1 |
| Szymonowicz, W | 1 |
| Fryburg, JS | 1 |
| Greer, KE | 1 |
| Vanderhooft, SL | 1 |
| Stephan, MJ | 1 |
| Cambiaghi, S | 1 |
| Tadini, G | 1 |
| Barbareschi, M | 1 |
| Menni, S | 1 |
| Caputo, R | 1 |
| Tsao, CY | 1 |
| Sommer, A | 1 |
| Hamoudi, AB | 1 |
| Zoll, B | 1 |
| Wolf, J | 1 |
| Lensing-Hebben, D | 1 |
| Pruggmayer, M | 1 |
| Thorpe, B | 1 |
| Seaver, LH | 1 |
| Joffe, L | 1 |
| Spark, RP | 1 |
| Smith, BL | 1 |
| Hoyme, HE | 2 |
| Poole, MD | 1 |
| Striano, S | 1 |
| Ruosi, P | 1 |
| Guzzetta, V | 1 |
| Perone, L | 1 |
| Manto, A | 1 |
| Cirillo, S | 1 |
| Chang, GY | 1 |
| Schirren, CG | 1 |
| Wörle, B | 1 |
| Kind, P | 1 |
| Plewig, G | 1 |
| Martínez-Frías, ML | 1 |
| Arroyo Carrera, I | 1 |
| Muñoz-Delgado, NJ | 1 |
| Nieto Conde, C | 1 |
| Rodríguez-Pinilla, E | 1 |
| Urioste Azcorra, M | 1 |
| Omeñaca Teres, F | 1 |
| García Alix, A | 1 |
| Tay, YK | 1 |
| Weston, WL | 1 |
| Ganong, CA | 1 |
| Klingensmith, GJ | 1 |
| Shields, JA | 2 |
| Shields, CL | 2 |
| Eagle, RC | 2 |
| Arevalo, F | 1 |
| De Potter, P | 1 |
| Narbay, G | 1 |
| Meire, F | 1 |
| Verloes, A | 1 |
| Casteels, I | 1 |
| Devos, E | 1 |
| Arevalo, JF | 1 |
| DePotter, P | 1 |
| Legius, E | 1 |
| Demaerel, P | 1 |
| van den Berghe, H | 5 |
| Plessis, G | 1 |
| Le Treust, M | 1 |
| Le Merrer, M | 2 |
| Pousti, TJ | 1 |
| Bartlett, RA | 1 |
| Puig, L | 1 |
| Nadal, C | 1 |
| Fernández-Figueras, MT | 1 |
| Alegre, M | 1 |
| de Moragas, JM | 1 |
| Allbritton, J | 1 |
| Simmons-O'Brien, E | 1 |
| Hutcheons, D | 1 |
| Whitmore, SE | 1 |
| Farah, S | 1 |
| Farag, T | 1 |
| Sabry, MA | 1 |
| Simeonov, ST | 1 |
| al-Khattam, S | 1 |
| Abulhassan, SJ | 1 |
| Quasrawi, B | 1 |
| al-Busairi, W | 1 |
| al-Awadi, SA | 1 |
| Moerman, P | 1 |
| Wilson, C | 1 |
| Aftimos, S | 1 |
| Pereira, A | 1 |
| McKay, R | 1 |
| Klinger, G | 1 |
| Merlob, P | 1 |
| Lin, AE | 1 |
| Westgate, MN | 1 |
| van der Velde, ME | 1 |
| Lacro, RV | 1 |
| Holmes, LB | 1 |
| Rybojad, M | 1 |
| Guibal, F | 1 |
| Vignon-Pennamen, MD | 1 |
| Prigent, F | 1 |
| Morel, P | 1 |
| Bourrat, E | 1 |
| Chapman, MS | 1 |
| Peraza, JE | 1 |
| Spencer, SK | 1 |
| Savarirayan, R | 1 |
| Thompson, EM | 1 |
| Abbott, KJ | 1 |
| Moore, MH | 1 |
| Tekin, M | 1 |
| Bodurtha, J | 1 |
| Ciftçi, E | 1 |
| Arsan, S | 1 |
| Diederen, PV | 1 |
| Van Neer, FJ | 1 |
| De Vries, L | 1 |
| Beemer, F | 1 |
| Van Vloten, WA | 1 |
| Picard, C | 1 |
| Couderc, S | 1 |
| Skojaei, T | 1 |
| Salomon, R | 1 |
| de Lonlay, P | 1 |
| Munnich, A | 1 |
| Keymolen, K | 1 |
| De Smet, L | 1 |
| Bracke, P | 1 |
| Sniderman, LC | 1 |
| Koenekoop, RK | 1 |
| O'Gorman, AM | 1 |
| Usher, RH | 1 |
| Sufrategui, MR | 1 |
| Moroz, B | 1 |
| Watters, GV | 1 |
| Der Kaloustian, VM | 2 |
| Hedstrand, H | 1 |
| Ekwall, O | 1 |
| Haavik, J | 1 |
| Landgren, E | 1 |
| Betterle, C | 1 |
| Perheentupa, J | 1 |
| Gustafsson, J | 1 |
| Husebye, E | 1 |
| Rorsman, F | 1 |
| Kämpe, O | 1 |
| Glaessl, A | 1 |
| Hohenlautner, U | 1 |
| Landthaler, M | 1 |
| Vogt, T | 1 |
| Woollons, A | 1 |
| Darley, CR | 1 |
| Lee, PJ | 1 |
| Brenton, DP | 1 |
| Sonksen, PH | 1 |
| Black, MM | 1 |
| Goucha, S | 1 |
| Fazaa, B | 1 |
| Ezzine, N | 1 |
| Jaber, K | 1 |
| Elandaloussi, H | 1 |
| Abid, R | 1 |
| Kamoun, MR | 1 |
| Amor, DJ | 2 |
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| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Genetic Disease Gene Identification[NCT00916903] | 200 participants (Anticipated) | Observational | 2005-10-31 | Enrolling by invitation | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
31 reviews available for salicylic acid and Syndrome
| Article | Year |
|---|---|
[Small retinal, cochlear, and cerebral infarctions in the young patient, "SICRET" syndrome of Susac syndrome].
Topics: Adult; Anticoagulants; Arterioles; Cerebral Infarction; Cochlea; Deafness; Diagnosis, Differential; | 1998 |
Graham-Little-Piccardi-Lasseur syndrome: case report and review of the syndrome in men.
Topics: Abnormalities, Multiple; Adult; Alopecia; Axilla; Cicatrix; Darier Disease; Eyebrows; Humans; Lichen | 2014 |
Neurocutaneous disease: Neurocutaneous dysesthesias.
Topics: Facial Dermatoses; Femoral Neuropathy; Humans; Nerve Compression Syndromes; Paresthesia; Pruritus; S | 2016 |
Amicrobial pustulosis of the folds: Where have we gone 25years after its original description?
Topics: Dermis; Diagnosis, Differential; Drug Therapy, Combination; Ear Canal; Glucocorticoids; Humans; Lupu | 2017 |
Finlay-Marks syndrome: another sporadic case and additional manifestations.
Topics: Abnormalities, Multiple; Ear; Genes, Dominant; Humans; Hypospadias; Infant, Newborn; Male; Natal Tee | 2004 |
A case of Adams-Oliver syndrome with associated brain and pulmonary involvement: further evidence of vascular pathology?
Topics: Abnormalities, Multiple; Adult; Brain; Central Nervous System; Consanguinity; Female; Humans; Hypert | 2004 |
Hypothelia, syndactyly, and ear malformation--a variant of the scalp-ear-nipple syndrome?: Case report and review of the literature.
Topics: Abnormalities, Multiple; Adult; Ear; Female; Fingers; Humans; Karyotyping; Nipples; Scalp; Syndactyl | 2005 |
Association of Adams-Oliver syndrome with pulmonary arterio-venous malformation in the same family: a further support to the vascular hypothesis.
Topics: Abnormalities, Multiple; Adult; Arteriovenous Malformations; Child; Diagnosis, Differential; Endothe | 2005 |
Athelia: case report and review of the literature.
Topics: Adolescent; Choanal Atresia; Dermoid Cyst; Ear; Female; Humans; Nipples; Plastic Surgery Procedures; | 2005 |
[Johanson-Blizzard syndrome].
Topics: Abnormalities, Multiple; Child; Developmental Disabilities; Diagnosis, Differential; Female; Genetic | 2006 |
Congenital cardiac malformations in Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Alopecia; Child; Child, Preschool; Female; Heart Defects, Congenital; Human | 1995 |
Trisomy 13 (Patau syndrome) with an 11-year survival.
Topics: Abnormalities, Multiple; Adult; Brain; Child; Child, Preschool; Chromosomes, Human, Pair 13; Female; | 1993 |
Ophthalmic features of the organoid nevus syndrome.
Topics: Adolescent; Arachnoid Cysts; Cartilage; Child; Choristoma; Choroid; Coloboma; Eye Abnormalities; Fac | 1996 |
Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: another case of Finlay-Marks syndrome.
Topics: Abnormalities, Multiple; Adult; Ear; Face; Female; Hair; Humans; Kidney; Nipples; Scalp; Syndrome; T | 1997 |
Adams-Oliver syndrome: genetics and associated anomalies of cutis aplasia.
Topics: Abnormalities, Multiple; Aorta, Thoracic; Aortic Coarctation; Diseases in Twins; Ductus Arteriosus, | 1997 |
Report of two sibs with Knobloch syndrome (encephalocoele and viteroretinal degeneration) and other anomalies.
Topics: Abnormalities, Multiple; Encephalocele; Eye Abnormalities; Humans; Infant; Infant, Newborn; Lung; Ly | 1998 |
Adams-Oliver syndrome: autosomal recessive inheritance and new phenotypic-anthropometric findings.
Topics: Anthropometry; Body Weights and Measures; Foot Deformities, Congenital; Genes, Recessive; Genetic Di | 1998 |
Adams-Oliver syndrome associated with cardiovascular malformations.
Topics: Abnormalities, Multiple; Adult; Aortic Valve; Child, Preschool; Female; Fingers; Genes, Dominant; He | 1998 |
Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvement.
Topics: Abnormalities, Multiple; Adult; Ear; Face; Fathers; Female; Hand Deformities, Congenital; Humans; In | 1999 |
Knobloch syndrome involving midline scalp defect of the frontal region.
Topics: Abnormalities, Multiple; Child, Preschool; Craniofacial Abnormalities; Humans; Male; Scalp; Syndrome | 2000 |
Sporadic Bazex-Dupré-Christol-like syndrome: early onset basal cell carcinoma, hypohidrosis, hypotrichosis, and prominent milia.
Topics: Acneiform Eruptions; Adult; Carcinoma, Basal Cell; Female; Humans; Hypohidrosis; Hypotrichosis; Neop | 2000 |
An autopsy case of Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Abortion, Habitual; Abortion, Therapeutic; Adult; Autopsy; Female; Fetal Di | 2000 |
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
Topics: Abnormalities, Multiple; Consanguinity; Ectodermal Dysplasia; Epilepsy, Tonic-Clonic; Fingers; Growt | 2000 |
[Scalp-ear-nipple syndrome].
Topics: Ear, External; Female; Humans; Nipples; Scalp; Syndrome | 2001 |
[Limb and scalp defects, Adams-Oliver type].
Topics: Female; Humans; Limb Deformities, Congenital; Male; Scalp; Skull; Syndrome | 2001 |
Adams-Oliver syndrome revisited.
Topics: Female; Follow-Up Studies; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Infan | 1991 |
Congenital scalp and skull defects with terminal transverse limb anomalies (Adams-Oliver syndrome): report of three additional cases.
Topics: Family Health; Female; Foot Deformities, Congenital; Genes, Dominant; Humans; Infant, Newborn; Male; | 1990 |
[Clinical aspects and genetics of congenital skin defects].
Topics: Abnormalities, Multiple; Congenital Abnormalities; Humans; Infant, Newborn; Pedigree; Scalp; Skin Ab | 1988 |
Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature.
Topics: Female; Fingers; Humans; Infant, Newborn; Male; Pedigree; Scalp; Syndrome; Toes | 1988 |
Aplasia cutis congenita: a clinical review and proposal for classification.
Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Adult; Epidermolysis Bullosa; Female; Fetal De | 1986 |
Alopecia: syndromes of genetic significance.
Topics: Abnormalities, Multiple; Adolescent; Adult; Age Factors; Alopecia; Alopecia Areata; Child; Child, Pr | 1973 |
1 trial available for salicylic acid and Syndrome
| Article | Year |
|---|---|
Temporo-spatial correlations between scalp and centromedian thalamic EEG activities of stage II slow wave sleep in patients with generalized seizures of the cryptogenic Lennox-Gastaut syndrome.
Topics: Adolescent; Arousal; Cerebral Cortex; Child, Preschool; Electroencephalography; Epilepsy, Absence; F | 2002 |
158 other studies available for salicylic acid and Syndrome
| Article | Year |
|---|---|
Otological lesions in pachyonychia congenita syndrome.
Topics: Adult; Drug Therapy, Combination; Ear, External; Emollients; Humans; Keratolytic Agents; Keratosis; | 1996 |
Ectopic meningothelial hamartoma with spindled melanocytes, an unusual finding in a rare neoplasm.
Topics: Hamartoma; Humans; Melanocytes; Neoplasms; Scalp; Syndrome | 2022 |
Clark level could be still a useful prognostic marker in scalp melanoma: a multicentric cross-sectional study.
Topics: Cross-Sectional Studies; Humans; Melanoma; Prognosis; Scalp; Skin Neoplasms; Syndrome | 2022 |
Repigmentation of Scalp Hair: A Feature of Early Melanoma.
Topics: Hair; Humans; Melanoma; Scalp; Syndrome | 2023 |
[A scalp lesion].
Topics: Animals; Dermacentor; Female; Humans; Middle Aged; Neck; Scalp; Scalp Dermatoses; Spotted Fever Grou | 2020 |
Athena: Speciality Certificate Examination case for Paediatrics and Genetics: a case of brittle hair.
Topics: Child; Hair; Hair Diseases; Humans; Physical Examination; Scalp; Syndrome | 2022 |
Oesophageal epidermal naevi as a feature of systematised epidermal naevus syndrome.
Topics: Adult; Esophageal Neoplasms; Facial Neoplasms; Female; Humans; Nevus; Scalp; Syndrome; Tongue Neopla | 2018 |
Unusually extensive scalp ulcerations manifested in pemphigus erythematosus.
Topics: Autoimmune Diseases; Female; Humans; Lupus Erythematosus, Discoid; Pemphigus; Scalp; Scalp Dermatose | 2018 |
Trigeminal Trophic Syndrome-A Unique Clinical Presentation of a Rare Condition.
Topics: Female; Humans; Middle Aged; Rare Diseases; Scalp; Scalp Dermatoses; Skin Ulcer; Syndrome; Trigemina | 2019 |
Graham-Little-Piccardi-Lassueur syndrome.
Topics: Alopecia; Axilla; Cicatrix; Female; Groin; Hair Diseases; Humans; Middle Aged; Scalp; Syndrome | 2019 |
Trigeminal trophic syndrome: report of 3 cases affecting the scalp.
Topics: Aged; Delusions; Diagnosis, Differential; Female; Humans; Middle Aged; Parasitic Diseases; Scalp; Se | 2013 |
Epidermal nevus in association with some uncommon manifestations.
Topics: Consanguinity; DNA Mutational Analysis; Ectodermal Dysplasia; Female; Fractures, Bone; Head and Neck | 2013 |
Scalp eschar and neck lymphadenopathy after tick bite: an emerging syndrome with multiple causes.
Topics: Adolescent; Adult; Aged; Animals; Child; Child, Preschool; Dermacentor; Female; Humans; Lymphatic Di | 2014 |
[CO2 laser treatment of skin cylindromas in Brooke-Spiegler syndrome].
Topics: Adult; Age of Onset; Aged; Carcinoma, Adenoid Cystic; Female; Head and Neck Neoplasms; Humans; Laser | 2014 |
Sinking skin flap syndrome and paradoxical herniation secondary to lumbar drainage.
Topics: Adult; Aged; Brain; Cerebrospinal Fluid; Decompressive Craniectomy; Drainage; Female; Humans; Lumbar | 2015 |
Trigeminal trophic syndrome with histopathologic correlation.
Topics: Biopsy; Female; Herpes Zoster; Humans; Middle Aged; Nasal Cavity; Pain; Pruritus; Scalp; Syndrome; T | 2015 |
A case of Graham-Little-Piccardi-Lasseur syndrome.
Topics: Aged; Alopecia; Axilla; Female; Groin; Humans; Lichen Planus; Scalp; Syndrome | 2015 |
Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Brain; Dura Mater; Ectodermal Dysplasia; Fatal Outcome; Humans; Infant, New | 2008 |
Brooke-Spiegler syndrome complicated by unilateral hearing loss.
Topics: Adult; Carcinoma, Adenoid Cystic; Carcinoma, Skin Appendage; Ear Neoplasms; Hearing Loss, Unilateral | 2008 |
A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafness.
Topics: Abnormalities, Multiple; Case-Control Studies; DNA Mutational Analysis; Hearing Loss, Sensorineural; | 2009 |
Chin-sternum-heart syndrome type of injury observed in a pedestrian victim of car traffic accident.
Topics: Accidents, Traffic; Aorta; Central Nervous System Depressants; Chin; Ethanol; Forensic Pathology; Fr | 2009 |
A case of Adams-Oliver syndrome following in vitro fertilization.
Topics: Abnormalities, Multiple; Adult; Female; Fertilization in Vitro; Humans; Infant, Newborn; Limb Deform | 2009 |
Familial cylindromatosis and brooke-spiegler syndrome: a review of current therapeutic approaches and the surgical challenges posed by two affected families.
Topics: Carcinoma, Adenoid Cystic; Carcinoma, Skin Appendage; Family; Female; Genetic Predisposition to Dise | 2009 |
Adams-Oliver syndrome: Additions to the clinical features and possible role of BMP pathway.
Topics: Abnormalities, Multiple; Bone Morphogenetic Proteins; Child, Preschool; Female; Humans; Infant; Limb | 2009 |
Clinical lessons learned from the International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Cleft Lip; Cleft Palate; Ectode | 2009 |
Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Cleft Lip; Cleft Palate; Ectode | 2009 |
Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis.
Topics: Acrocephalosyndactylia; Case-Control Studies; Child, Preschool; Cluster Analysis; Craniosynostoses; | 2010 |
Transarterial embolization of a scalp hemangioma presenting with Kasabach-Merritt syndrome.
Topics: Blood Coagulation Disorders; Cerebral Angiography; Embolization, Therapeutic; Hemangioma; Humans; In | 2009 |
Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction.
Topics: Adolescent; Adult; Age Distribution; Age of Onset; Biopsy, Needle; Carcinoma, Adenoid Cystic; Child; | 2009 |
Management of large scalp and skull defects in a severe case of Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Bandages; Dura Mater; Ectodermal Dysplasia; Female; Hand Deformities, Conge | 2009 |
A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation.
Topics: Cochlear Implantation; Connexin 26; Connexins; Deafness; DNA Mutational Analysis; Female; Hearing Ai | 2010 |
New mutation in the CYLD gene within a family with Brooke-Spiegler syndrome.
Topics: Adenoma, Sweat Gland; Adolescent; Adult; Biopsy; Carcinoma, Adenoid Cystic; Carcinoma, Basal Cell; C | 2010 |
An unusual case of turban tumor syndrome treated with total scalp excision and advancement flap and skin graft reconstruction.
Topics: Adult; Carcinoma, Adenoid Cystic; Facial Neoplasms; Female; Humans; Neoplasms, Adnexal and Skin Appe | 2010 |
Dermal cylindroma of the scalp (turban tumour) and subjacent calvarian defects.
Topics: Aged; Angiography; Biopsy; Carcinoma, Adenoid Cystic; Carotid Arteries; Female; Head and Neck Neopla | 2010 |
Graham-Little syndrome.
Topics: Alopecia; Female; Glucocorticoids; Humans; Keratosis; Middle Aged; Prednisone; Scalp; Scalp Dermatos | 2010 |
Autosomal recessive type of Adams-Oliver syndrome: prenatal diagnosis.
Topics: Abortion, Induced; Autopsy; Chromosome Disorders; Consanguinity; Female; Genes, Recessive; Humans; L | 2002 |
[Rapp-Hodgkin's syndrome: two cases].
Topics: Adult; Child, Preschool; Craniofacial Abnormalities; Dermatitis; Ectodermal Dysplasia; Humans; Hypoh | 2003 |
An acromegaloid, cutis verticis gyrata, corneal leukoma syndrome. A new medical entity.
Topics: Acromegaly; Corneal Opacity; Dermatology; Humans; Scalp; Skin Diseases; Syndrome | 1962 |
[A true single cornu cutaneum].
Topics: Cornus; Humans; Neoplasms; Scalp; Syndrome | 1961 |
Aplasia cutis congenita, polythelia, microcephaly, and developmental delay: a unique expression of polytopic field defect involving possible 'paradominant' inheritance?
Topics: Abnormalities, Multiple; Child; Developmental Disabilities; Ectodermal Dysplasia; Genes, Dominant; H | 2004 |
Two brothers with trichiasis, entropion and corneal scarring, sensorineural hearing loss, progressive thinning of scalp hair, mild learning difficulties and distinct facial features. A new syndrome?
Topics: Adolescent; Alopecia; Entropion; Face; Hearing Loss, Sensorineural; Humans; Male; Scalp; Siblings; S | 2004 |
Oculo-ectodermal syndrome: a new tumour predisposition syndrome.
Topics: Alopecia; Child, Preschool; Female; Follow-Up Studies; Genetic Predisposition to Disease; Granuloma, | 2004 |
Case 3. Brooke-Spiegler syndrome.
Topics: Adenoma; Aged; Facial Neoplasms; Female; Head and Neck Neoplasms; Humans; Neoplasms, Basal Cell; Neo | 2004 |
Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Coronary Stenosis; Fatal Outcome; Fetal Growth Retardation; Heart Defects, | 2004 |
Johanson-blizzard syndrome: loss of glucagon secretion response to insulin-induced hypoglycemia.
Topics: Abnormalities, Multiple; Consanguinity; Exocrine Pancreatic Insufficiency; Failure to Thrive; Glucag | 2004 |
Sotos syndrome: surgical correction of abnormal craniofacial features.
Topics: Bone Transplantation; Child; Child, Preschool; Comorbidity; Craniofacial Abnormalities; Developmenta | 2005 |
Adams-Oliver syndrome and hepatoportal sclerosis: occasional association or common mechanism?
Topics: Abnormalities, Multiple; Child; Child, Preschool; Female; Foot Deformities, Congenital; Hand Deformi | 2005 |
Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre.
Topics: Adolescent; Adult; Age Distribution; Child; Child, Preschool; Ectodermal Dysplasia; Hair; Hair Disea | 2005 |
Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndrome.
Topics: Abnormalities, Multiple; Child; Ear; Humans; Karyotyping; Male; Nipples; Scalp; Syndrome | 2006 |
Association of Adams-Oliver syndrome and hepatoportal sclerosis: an additional case.
Topics: Abnormalities, Multiple; Child, Preschool; Foot Deformities, Congenital; Hand Deformities, Congenita | 2006 |
Extraocular sebaceous carcinoma in Muirr Torre Syndrome with unfavorable prognosis.
Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Colonic Neoplasms; Fatal Outcome; Female; Hum | 2006 |
Adams-Oliver syndrome: a case with complete expression.
Topics: Female; Humans; Infant, Newborn; Limb Deformities, Congenital; Scalp; Skull; Syndrome; Telangiectasi | 2006 |
Pemphigus vulgaris in a patient with 1p36 deletion syndrome.
Topics: Adult; Chromosome Deletion; Chromosomes, Human, Pair 1; Female; Humans; Pemphigus; Scalp; Syndrome | 2006 |
Norwegian scabies mimicking onychomycosis and scalp dermatitis in a child with IPEX syndrome.
Topics: Child, Preschool; Dermatitis; Diagnosis, Differential; Endocrine System Diseases; Forkhead Transcrip | 2007 |
Metastatic angiosarcoma of the scalp causing Kasabach-Merritt syndrome.
Topics: Aged; Fatal Outcome; Head and Neck Neoplasms; Hemangioma, Capillary; Hemangiosarcoma; Humans; Male; | 2007 |
Brooke-Spiegler syndrome.
Topics: Carcinoma, Adenoid Cystic; Diagnosis, Differential; Face; Female; Humans; Middle Aged; Scalp; Skin N | 2007 |
Lassueur-Graham-Little-Piccardi syndrome.
Topics: Alopecia; Axilla; Biopsy; Cicatrix; Diagnosis, Differential; Follow-Up Studies; Humans; Male; Middle | 2007 |
Aplasia cutis associated with coarctation of the aorta: could this be an incomplete form of Adams-Oliver syndrome?
Topics: Abnormalities, Multiple; Aortic Coarctation; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; | 2007 |
Adams-Oliver syndrome: congenital disease with gait disorder: a case report.
Topics: Abnormalities, Multiple; Child, Preschool; Humans; Limb Deformities, Congenital; Male; Movement Diso | 2007 |
Dense array EEG: methodology and new hypothesis on epilepsy syndromes.
Topics: Adolescent; Adult; Brain Mapping; Cerebral Cortex; Diagnosis, Computer-Assisted; Electrodes; Electro | 2008 |
[Spiegler carcinomas with associated symptoms. A new syndrome? (author's transl)].
Topics: Abnormalities, Multiple; Aged; Carcinoma, Adenoid Cystic; Female; Fingers; Humans; Nails, Malformed; | 1980 |
An association of subtotal cerebellar agenesis with organoid nevus--a possible new variety of neurocutaneous syndrome.
Topics: Adolescent; Cerebellum; Electronystagmography; Female; Humans; Intellectual Disability; Nevus; Nysta | 1983 |
In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequence.
Topics: Adult; Anencephaly; Brain; Cranial Sutures; Female; Gestational Age; Humans; Hydranencephaly; Infant | 1984 |
Anomalous cerebral venous drainage in Aarskog syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Cerebral Angiography; Child; Female; Genes, Recessive; G | 1984 |
Encephalocraniocutaneous lipomatosis: a recently described neurocutaneous syndrome.
Topics: Arachnoid; Brain Neoplasms; Cysts; Eyelid Neoplasms; Humans; Lipomatosis; Male; Scalp; Skin Neoplasm | 1984 |
Unexplained diarrhoea and failure to thrive in 2 siblings with unusual facies and abnormal scalp hair shafts: a new syndrome.
Topics: Amino Acids; Diarrhea, Infantile; Face; Female; Hair; Humans; Infant Nutrition Disorders; Infant, Ne | 1982 |
Picture of the mouth. Encephalocraniocutaneous lipomatosis.
Topics: Brain; Child; Choristoma; Eye Neoplasms; Hamartoma; Humans; Lipomatosis; Male; Scalp; Sclera; Skin N | 1982 |
Tumor conference #44. Carcinoma with sebaceous gland differentiation in the skin of a patient with possible Torre's syndrome.
Topics: Adenocarcinoma; Biopsy; Humans; Male; Middle Aged; Scalp; Sebaceous Gland Neoplasms; Skin Neoplasms; | 1982 |
Eosinophilic cellulitis. (Well's syndrome) in a child.
Topics: Alopecia; Cellulitis; Child; Dermatitis; Eosinophilia; Granuloma; Humans; Male; Scalp; Skin; Syndrom | 1981 |
The spectrum of frontonasal dysplasia in an inbred pedigree.
Topics: Consanguinity; Craniofacial Dysostosis; Face; Female; Humans; Hypertelorism; Infant, Newborn; Male; | 1980 |
[Schimmelpenning-Feuerstein-Mims syndrome (SFM syndrome)].
Topics: Aged; Carcinoma, Basal Cell; Cell Transformation, Neoplastic; Conjunctival Neoplasms; Diagnosis, Dif | 1994 |
Scalp-ear-nipple syndrome: additional manifestations.
Topics: Abnormalities, Multiple; Adult; Breast; Ear; Ectodermal Dysplasia; Female; Humans; Male; Nipples; Pe | 1994 |
Adams Oliver syndrome: a family with extreme variability in clinical expression.
Topics: Abnormalities, Multiple; Adult; Brain; Bronchi; Epilepsy; Female; Heart Defects, Congenital; Humans; | 1994 |
Adams-Oliver syndrome: a case with juvenile chronic myelogenous leukemia and chylothorax.
Topics: Chylothorax; Heart Defects, Congenital; Humans; Infant, Newborn; Leukemia, Myelogenous, Chronic, BCR | 1993 |
Epidermal naevi and bullous aplasia cutis congenita in a neonate.
Topics: Ectodermal Dysplasia; Humans; Infant, Newborn; Male; Nevus, Pigmented; Scalp; Skin Diseases, Vesicul | 1993 |
Severe skin erosions and scalp infections in AEC syndrome.
Topics: Abnormalities, Multiple; Child; Cleft Lip; Cleft Palate; Ectodermal Dysplasia; Eyelids; Female; Huma | 1993 |
Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity?
Topics: Cleft Palate; Ectodermal Dysplasia; Eyelids; Face; Hair; Humans; Infant; Male; Nails, Malformed; Oro | 1994 |
Aicardi syndrome, metastatic angiosarcoma of the leg, and scalp lipoma.
Topics: Eye Abnormalities; Female; Hemangioma, Cavernous; Hemangiosarcoma; Humans; Infant; Leg; Lipoma; Neop | 1993 |
Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch syndrome.
Topics: Child; Child, Preschool; Eye Diseases; Female; Genes, Recessive; Humans; Male; Myopia; Retinal Degen | 1993 |
Surgical caution with Carpenter's syndrome.
Topics: Acrocephalosyndactylia; Blood Loss, Surgical; Child, Preschool; Cranial Sinuses; Frontal Bone; Human | 1993 |
Cutis verticis gyrata--mental deficiency syndrome: a patient with drug-resistant epilepsy and polymicrogyria.
Topics: Adult; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 3; Epilepsy; Humans; Intellectual Disab | 1996 |
Cutis verticis gyrata, underrecognized neurocutaneous syndrome.
Topics: Adult; Epilepsy; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Scalp; Syndrome | 1996 |
A nevoid plaque with histological changes of trichoepithelioma and cylindroma in Brooke-Spiegler syndrome. An immunohistochemical study with cytokeratins.
Topics: Antibodies, Monoclonal; Carcinoma, Adenoid Cystic; Eyebrows; Female; Humans; Immunohistochemistry; K | 1995 |
[The Adams-Oliver syndrome in Spain: the epidemiological aspects].
Topics: Abnormalities, Multiple; Diagnosis, Differential; Ectodermal Dysplasia; Female; Humans; Infant, Newb | 1996 |
Epidermal nevus syndrome: association with central precocious puberty and woolly hair nevus.
Topics: Child, Preschool; Female; Hair Diseases; Humans; Nevus, Pigmented; Puberty, Precocious; Scalp; Skin | 1996 |
Ocular manifestations in Delleman syndrome (Oculocerebrocutaneous syndrome, OCC-syndrome) and encephalocraniocutaneous lipomatosis (ECCL). Report of three cases.
Topics: Abnormalities, Multiple; Brain; Child, Preschool; Eye Abnormalities; Face; Humans; Infant, Newborn; | 1996 |
Ocular manifestations of the organoid nevus syndrome.
Topics: Adolescent; Arachnoid Cysts; Cartilage; Child; Choristoma; Choroid; Coloboma; Eye Abnormalities; Fac | 1997 |
Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hypoplasia of the left arteria cerebri media. Further evidence that interruption of early embryonic blood supply may result in Adams-Oliver (plus) syndrome.
Topics: Abnormalities, Multiple; Anencephaly; Cerebral Arteries; Diagnostic Errors; Embryo, Mammalian; Foot | 1996 |
Brooke-Spiegler syndrome variant: segregation of tumor types with mixed differentiation in two generations.
Topics: Adult; Biopsy; Carcinoembryonic Antigen; Carcinoma, Adenoid Cystic; Facial Neoplasms; Female; Hair; | 1998 |
Cronkhite-Canada syndrome: report of two cases, biopsy findings in the associated alopecia, and a new treatment option.
Topics: Aged; Alopecia; Female; Glucocorticoids; Humans; Intestinal Polyps; Nail Diseases; Prednisone; Ranit | 1998 |
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findings.
Topics: Adult; Brain; Chromosome Inversion; Epilepsy; Humans; Intellectual Disability; Magnetic Resonance Im | 1998 |
Scalp defects in Fryns syndrome.
Topics: Abnormalities, Multiple; Fetus; Humans; Scalp; Skull; Syndrome | 1998 |
[Eosinophilic pustulosis in an infant accompanied by immune deficit].
Topics: Adult; Biopsy; Child; Child, Preschool; Eosinophilia; Eosinophils; Folliculitis; Humans; Immunologic | 1999 |
Parry-Romberg syndrome with contralateral and ipsilateral extremity involvement.
Topics: Adipose Tissue; Extremities; Facial Hemiatrophy; Female; Humans; Middle Aged; Scalp; Syndrome | 1999 |
Cerebral cortical dysplasia and digital constriction rings in Adams-Oliver syndrome.
Topics: Cerebral Cortex; Child, Preschool; Constriction, Pathologic; Female; Fingers; Genes, Dominant; Human | 1999 |
Further family with possible autosomal recessive inheritance of Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Adult; Child; Consanguinity; Family Health; Fatal Outcome; Female; Genes, R | 1999 |
[Cutis verticis gyrata].
Topics: Abnormalities, Multiple; Female; Humans; Infant; Karyotyping; Magnetic Resonance Imaging; Retinal Di | 1999 |
The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanism.
Topics: Abnormalities, Multiple; Brain Diseases; Constriction, Pathologic; Cysts; Face; Female; Fingers; Foo | 1999 |
Identification of tyrosine hydroxylase as an autoantigen in autoimmune polyendocrine syndrome type I.
Topics: Alopecia Areata; Autoantibodies; Autoantigens; Europe; Gene Library; Humans; Isoenzymes; Polyendocri | 2000 |
Cutis verticis gyrata of the scalp in a patient with autosomal dominant insulin resistance syndrome.
Topics: Adult; Biopsy; Female; Humans; Hyperinsulinism; Insulin Resistance; Scalp; Scalp Dermatoses; Syndrom | 2000 |
[GAPO syndrome].
Topics: Alopecia; Anodontia; Child; Dilatation, Pathologic; Facies; Growth Disorders; Hemangioma; Hernia, Um | 2000 |
Polymicrogyria associated with scalp and limb defects: variant of Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Brain; Child; Child, Preschool; Consanguinity; Female; Genes, Recessive; Hu | 2000 |
Encephalocraniocutaneous lipomatosis (Fishman syndrome): a rare neurocutaneous syndrome.
Topics: Brain; Calcinosis; Cerebral Cortex; Dermoid Cyst; Eye Diseases; Humans; Infant; Lipomatosis; Magneti | 2000 |
Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate gene.
Topics: Adult; Blepharoptosis; Child, Preschool; Dwarfism; Ear; Female; Guanine Nucleotide Exchange Factors; | 2001 |
MCA/MR syndrome with occipital scalp defect and valvular pulmonary stenosis: a cryptic 7pter duplication/18qter deficiency.
Topics: Child; Child, Preschool; Chromosomes, Human, Pair 18; Chromosomes, Human, Pair 7; Humans; Intellectu | 2001 |
[Systematic sebaceous nevus with multiple secondary tumors as the chief symptom of Schimmelpenning-Feuerstein-Mims syndrome].
Topics: Adenoma, Sweat Gland; Aged; Biopsy; Carcinoma, Basal Cell; Cell Transformation, Neoplastic; Diagnosi | 2001 |
Graham Little-Piccardi-Lassueur syndrome: effective treatment with cyclosporin A.
Topics: Alopecia; Axilla; Back; Cyclosporine; Erythema; Female; Humans; Immunosuppressive Agents; Middle Age | 2001 |
Scalp defects, polythelia, microcephaly, and developmental delay: a new syndrome with apparent autosomal dominant inheritance.
Topics: Abnormalities, Multiple; Adult; Child; Child, Preschool; Developmental Disabilities; Family Health; | 2002 |
Subcutaneous bone formation in the naevoid basal-cell carcinoma syndrome: normal urinary cyclic AMP response to parathyroid hormone infusion.
Topics: Adult; Bone Cysts; Calcium; Carcinoma, Basal Cell; Creatinine; Cyclic AMP; Humans; Jaw Diseases; Mal | 1975 |
Cutaneous vascular tumors.
Topics: Child, Preschool; Female; Hemangioma; Humans; Infant; Klippel-Trenaunay-Weber Syndrome; Leg; Lymphan | 1975 |
Congenital scalp defect with distal limb reduction anomalies.
Topics: Abnormalities, Multiple; Adult; Fingers; Genetic Counseling; Humans; Male; Scalp; Skull; Syndactyly; | 1977 |
Linear nevus sebaceous syndrome: neurological aspects documented by brain scans correlated with developmental history and radiographic studies.
Topics: Brain Diseases; Child; Female; Humans; Intellectual Disability; Nevus; Scalp; Sebaceous Gland Neopla | 1978 |
Congenital scalp defects associated with postaxial polydactyly.
Topics: Adult; Female; Fingers; Genes, Dominant; Humans; Infant, Newborn; Male; Pedigree; Scalp; Syndrome | 1979 |
Autosomal dominant inheritance of scalp defects with ectrodactyly.
Topics: Adolescent; Adult; Chromosome Aberrations; Chromosome Disorders; Female; Foot Deformities, Congenita | 1979 |
Autosomal dominantly inherited cutis aplasia congenita, ear malformations, right-sided facial paresis, and dermal sinuses.
Topics: Adult; Child; Child, Preschool; Ear, External; Facial Paralysis; Female; Genes, Dominant; Humans; Ma | 1979 |
An hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples.
Topics: Abnormalities, Multiple; Aged; Breast; Ear, External; Female; Humans; Male; Middle Aged; Nipples; Pe | 1978 |
Hereditary aplasia cutis congenita and associated defects. Three instances in one family and a survey of reported cases.
Topics: Adolescent; Adult; Humans; Infant; Infant, Newborn; Male; Scalp; Skull; Syndrome; Toes | 1977 |
Bilateral scalp necrosis in temporal arteritis. A rare complication of Horton's disease.
Topics: Aged; Giant Cell Arteritis; Humans; Male; Necrosis; Scalp; Syndrome | 1976 |
Skin thickness in cutis verticis gyrata and mental retardation syndrome.
Topics: Adult; Female; Humans; Hypertrophy; Intellectual Disability; Male; Scalp; Skin Diseases; Skinfold Th | 1976 |
The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs.
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Clubfoot; E | 1975 |
Phenotypic heterogeneity among the pilosebaceous dysplasias.
Topics: Adolescent; Alopecia; Child; Ectodermal Dysplasia; Female; Hair; Humans; Male; Orofaciodigital Syndr | 1975 |
[The linear sebaceous nevus syndrome. Feuerstein-Mims' syndrome].
Topics: Adolescent; Alopecia; Epilepsy; Humans; Male; Neck; Nevus; Scalp; Sebaceous Gland Neoplasms; Syndrom | 1975 |
Origin and relevance of aberrant scalp and upper facial hair patterning.
Topics: Eyebrows; Face; Hair; Humans; Scalp; Syndrome | 1975 |
Multifocal aplasia cutis congenita, distal limb hemimelia, and cutis marmorata telangiectatica in a patient with Adams-Oliver syndrome.
Topics: Abnormalities, Multiple; Ectodermal Dysplasia; Humans; Infant; Leg; Male; Scalp; Skin; Syndrome; Tel | 1992 |
Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.
Topics: Abnormalities, Multiple; Cleft Lip; Cleft Palate; Humans; Hypertelorism; Hypospadias; Infant; Male; | 1992 |
Keratosis follicularis spinulosa decalvans: report of a case with ultrastructural study and unsuccessful trial of retinoids.
Topics: Biopsy; Darier Disease; Etretinate; Humans; Infant; Male; Microscopy, Electron; Scalp; Scalp Dermato | 1992 |
Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome: an additional clinical observation.
Topics: Abnormalities, Multiple; Child; Female; Genes, Dominant; Humans; Limb Deformities, Congenital; Male; | 1992 |
Adams-Oliver syndrome associated with congenital heart defect: not a coincidence.
Topics: Fingers; Heart Defects, Congenital; Humans; Infant, Newborn; Male; Scalp; Syndrome; Toes | 1991 |
Vascular abnormalities in epidermal nevus syndrome.
Topics: Adolescent; Adult; Cerebral Infarction; Child; Child, Preschool; Humans; Male; Nevus, Pigmented; Sca | 1991 |
The Rapp-Hodgkin syndrome.
Topics: Adult; Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Male; Microscopy, Electron, Scanning; | 1991 |
Buschke-Ollendorff syndrome of the scalp: histologic and ultrastructural findings.
Topics: Collagen; Elastic Tissue; Fibrosis; Humans; Male; Middle Aged; Nevus; Osteopoikilosis; Pedigree; Sca | 1991 |
Thrombocytopenia-absent radii syndrome and lack of response to the pulsed dye laser.
Topics: Arteriovenous Malformations; Face; Humans; Infant; Laser Therapy; Male; Neck; Radius; Scalp; Syndrom | 1990 |
[Plicate pachyderma of the head].
Topics: Adult; Biopsy; Humans; Male; Osteoarthropathy, Primary Hypertrophic; Scalp; Scalp Dermatoses; Syndro | 1990 |
Juvenile hyaline fibromatosis (Murray-Puretic-Drescher syndrome): oral and systemic findings in siblings.
Topics: Child, Preschool; Facial Neoplasms; Fibroma; Fibromatosis, Gingival; Foot; Forehead; Humans; Hyalin; | 1986 |
Johanson-Blizzard syndrome: clinical and pathological findings in 2 sibs.
Topics: Abnormalities, Multiple; Autopsy; Follow-Up Studies; Humans; Infant, Newborn; Islets of Langerhans; | 1989 |
Nevus sebaceus associated with major ophthalmologic abnormalities.
Topics: Adolescent; Choristoma; Choroid; Coloboma; Eye Abnormalities; Female; Humans; Intellectual Disabilit | 1987 |
Torre-Muir syndrome. An association with isolated sebaceous carcinoma.
Topics: Abdominal Muscles; Adenocarcinoma; Aged; Carcinoma, Squamous Cell; Female; Humans; Lymphatic Metasta | 1985 |
Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
Topics: Abnormalities, Multiple; Adult; Dermatoglyphics; Genes, Recessive; Humans; Limb Deformities, Congeni | 1988 |
Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome?
Topics: Abnormalities, Multiple; Blood Vessels; Heart Defects, Congenital; Humans; Limb Deformities, Congeni | 1988 |
[A case of Gottron reticulosarcomatosis of the skin].
Topics: Aged; Facial Neoplasms; Humans; Lymphatic Metastasis; Lymphoma, Large B-Cell, Diffuse; Male; Scalp; | 1986 |
Encephalocraniocutaneous lipomatosis.
Topics: Adolescent; Brain Neoplasms; Cerebral Angiography; Eye Neoplasms; Facial Neoplasms; Female; Humans; | 1987 |
Nevus sebaceus of Jadassohn: the head and neck manifestations.
Topics: Adolescent; Child; Female; Hamartoma; Head and Neck Neoplasms; Humans; Infant; Nevus; Scalp; Sebaceo | 1987 |
Congenital scalp defects with distal limb reduction anomalies.
Topics: Abnormalities, Multiple; Fingers; Genes, Dominant; Genetic Variation; Humans; Scalp; Skull; Syndrome | 1987 |
[Johanson-Blizzard syndrome].
Topics: Abnormalities, Multiple; Clinical Enzyme Tests; Exocrine Pancreatic Insufficiency; Female; Hair; Hum | 1986 |
The Johanson-Blizzard syndrome: a second report of full autopsy findings.
Topics: Abnormalities, Multiple; Brain; Female; Humans; Infant; Malabsorption Syndromes; Nose; Pancreas; Sca | 1987 |
Cutaneous, ocular, and osteoarticular candidiasis in heroin addicts: new clinical and therapeutic aspects in 38 patients.
Topics: Adult; Aged; Amphotericin B; Bone Diseases; Candida albicans; Candidiasis; Candidiasis, Cutaneous; E | 1985 |
Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance.
Topics: Adolescent; Fingers; Genes, Dominant; Humans; Intellectual Disability; Male; Radiography; Scalp; Sku | 1985 |
Terminal transverse defects with aplasia cutis congenita (Adams-Oliver syndrome).
Topics: Abnormalities, Multiple; Female; Fingers; Genes, Dominant; Humans; Infant, Newborn; Pedigree; Scalp; | 1985 |
[On the Schimmelpenning-Feuerstein-Mims-syndrome (Organoid Nevus-Phakomatosis) (author's transl)].
Topics: Child; Follow-Up Studies; Head and Neck Neoplasms; Humans; Male; Neurofibromatosis 1; Nevus, Pigment | 1974 |
[Follicular mucinosis and large area, partly lichenoid, partly sclerodermiform generalized paramyloidosis as a cutaneous paraneoplastic syndrome in myeloma (IgD and light chain plasmacytoma)].
Topics: Alopecia; Amyloidosis; Blood Proteins; Drug Therapy, Combination; Eye Manifestations; Humans; Immuno | 1974 |
[Case presentations].
Topics: Abdomen; Adolescent; Angiokeratoma; Argyria; Child; Child, Preschool; Female; Fingers; Hair; Humans; | 1974 |
Linear sebaceous nevus syndrome.
Topics: Head and Neck Neoplasms; Humans; Nevus, Pigmented; Scalp; Sebaceous Glands; Skin Neoplasms; Syndrome | 1972 |
Focal dermal hypoplasia. A nine-year follow-up study.
Topics: Abnormalities, Multiple; Anophthalmos; Atrophy; Buttocks; Child; Dental Enamel Hypoplasia; Face; Fem | 1973 |
[Jadassohn's sebacous gland nevus and basal cell carcinoma].
Topics: Adult; Carcinoma, Basal Cell; Head and Neck Neoplasms; Humans; Male; Nevus, Pigmented; Precancerous | 1973 |
The electrophoretic pattern of cerebrospinal fluid proteins in the cutis verticis gyrata and mental retardation syndrome.
Topics: Adolescent; Adult; Albumins; Blood Protein Electrophoresis; Cerebral Palsy; Cerebral Ventricles; Cer | 1974 |
[Facial deformities in the tricho-rhino-phalangeal syndrome].
Topics: Abnormalities, Multiple; Face; Fingers; Hair; Humans; Nose Deformities, Acquired; Rhinoplasty; Scalp | 1974 |
Intestinal and cutaneous haemangiomatosis.
Topics: Adolescent; Cecal Neoplasms; Child; Child, Preschool; Colonic Neoplasms; Foot Diseases; Hemangioma, | 1974 |
[Solomon's epidermic nevus syndrome].
Topics: Abnormalities, Multiple; Adult; Bone and Bones; Conjunctiva; Eye Neoplasms; Female; Humans; Nevus; P | 1974 |